USP2 Attenuates Spermatogenic Cell Apoptosis Via PINK1/Parkin-Dependent Mitophagy in Varicocoele: A Functional Study.

IF 3.4 2区 医学 Q1 ANDROLOGY
Andrology Pub Date : 2026-09-01 Epub Date: 2026-04-10 DOI:10.1111/andr.70230
Rui-Jie Yao, Hong Xiao, Jun-Hang Zheng, Bin Lin, Shi-Jie Liao, Hao-Han He, Ning Xu, Hui-Liang Zhou
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引用次数: 0

Abstract

Background: Varicocoele is a major cause of male infertility, yet its underlying molecular mechanisms and determinants of surgical efficacy remain unclear.

Objective: This study aimed to identify key proteins involved in varicocoele-related infertility and to investigate the expression and functional role of ubiquitin-specific peptidase 2 in spermatozoa and spermatogenic cells.

Methods: Ubiquitin-specific peptidase 2 expression in spermatozoa from varicocoele patients was analyzed before and after varicocelectomy by Western blotting. In vitro, ubiquitin-specific peptidase 2 was overexpressed or silenced in mouse GC-2 spermatocyte cells to assess mitochondrial autophagy (PINK1/Parkin pathway), autophagic flux, apoptosis, and reactive oxygen species. In vivo, a left-sided varicocoele rat model was established, and ubiquitin-specific peptidase 2 activity was inhibited by intratesticular injection of ML364. Testicular histopathology and sperm motility were evaluated.

Results: Ubiquitin-specific peptidase 2 protein expression was significantly reduced in spermatozoa after varicocelectomy. Ubiquitin-specific peptidase 2 overexpression enhanced PINK1/Parkin-mediated mitochondrial autophagy and protected spermatogenic cells from apoptosis, whereas ubiquitin-specific peptidase 2 knockdown impaired mitochondrial autophagy and increased cell apoptosis. In varicocoele rats, ubiquitin-specific peptidase 2 inhibition aggravated seminiferous tubule damage, reduced spermatogenic cell density, and impaired sperm motility. In human spermatozoa, ML364 treatment significantly decreased progressive motility without affecting sperm concentration.

Conclusion: Ubiquitin-specific peptidase 2 is essential for maintaining mitochondrial quality control and spermatogenic cell survival in varicocoele by regulating PINK1/Parkin-mediated autophagy and oxidative stress, highlighting its potential as a biomarker and therapeutic target for varicocoele-related male infertility.

USP2通过PINK1/ parkin依赖性线粒体自噬在精索静脉曲张中减弱生精细胞凋亡:一项功能研究
背景:精索静脉曲张是男性不育的主要原因,但其潜在的分子机制和手术疗效的决定因素尚不清楚。目的:本研究旨在鉴定精索静脉曲张相关性不孕的关键蛋白,探讨泛素特异性肽酶2在精子和生精细胞中的表达及其功能作用。方法:应用免疫印迹法分析精索静脉曲张切除术前后患者精子中泛素特异性肽酶2的表达。在体外,泛素特异性肽酶2在小鼠GC-2精母细胞中过表达或沉默,以评估线粒体自噬(PINK1/Parkin通路)、自噬通量、凋亡和活性氧。在体内,建立左侧精索静脉曲张大鼠模型,睾丸内注射ML364抑制泛素特异性肽酶2活性。评估睾丸组织病理学和精子活力。结果:精索静脉曲张切除术后精子中泛素特异性肽酶2蛋白表达明显降低。泛素特异性肽酶2过表达可增强PINK1/ parkin介导的线粒体自噬并保护生精细胞免于凋亡,而泛素特异性肽酶2敲低可损害线粒体自噬并增加细胞凋亡。在精索静脉曲张大鼠中,泛素特异性肽酶2抑制加重了精管损伤,降低了生精细胞密度,损害了精子活力。在人类精子中,ML364处理显著降低了进行性运动,但不影响精子浓度。结论:泛素特异性肽酶2通过调节PINK1/ parkin介导的自噬和氧化应激,对维持精索静脉曲张患者线粒体质量控制和生精细胞存活至关重要,这凸显了其作为精索静脉曲张相关男性不育症的生物标志物和治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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